Acumatch A Series 132-28-06Recalls & reported problems

Summary

The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 10885862023018), received between Jun 19, 2020 and Feb 3, 2026 — classified as 5 injuries.

The most frequently reported specific device problem is “Naturally Worn” (5 reports).

1 FDA recall record name this device's identifier, 1 still open.

1 other recall cover devices cleared under the same FDA submission (K993082); they may or may not involve this specific model.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Recalls naming this device

1. Aug 11, 2022Class IIOpen, Classified

   Specific GXL acetabular polyethylene liners, packaged in non-conforming bags, may adversely impact the device and contribute to accelerated wear.

   Z-1734-2022 · Root cause: Process control · Recall details · FDA record ↗

Most reported problems

Recent adverse event reports

The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.

• InjuryFeb 3, 2026Device Dislodged or Dislocated; Naturally Worn

  IT WAS REPORTED THAT A PATIENT, WHO HAD A THA, UNDERWENT A REVISION PROCEDURE APPROXIMATELY 19 YEARS 5 MONTHS POST THE INITIAL PROCEDURE. THE PATIENT WAS REVISED DUE TO EXPECTED WEAR AND REPORTS OF DISLOCATION. THE HEAD LINER WAS EXCHANGED. IT WAS STATED THERE WERE NO ISSUES WITH THE SURGERY. THE EXPLANTED DEVICE IS NOT AVAILABLE FOR RETURN. AN X-RAY WAS PROVIDED. NO FURTHER INFORMATION.

  Patient problems: Joint Dislocation

  MAUDE report 24251567 ↗
• InjurySep 18, 2025Naturally Worn; Naturally Worn

  AS REPORTED, APPROXIMATELY 20 YEARS AND 6 MONTHS POST THE INITIAL TOTAL HIP REPLACEMENT, THE PATIENT WAS REVISED DUE TO PAIN AND WEAR. THE PATIENT WAS CONVERTED TO A COMPETITOR CUP AND DUAL MOBILITY LINER. A NEW EXACTECH HEAD WAS PLACED. THERE WERE NO ISSUES WITH THE SURGERY. NO FURTHER INFORMATION PROVIDED.

  Patient problems: Pain

  MAUDE report 23083103 ↗
• InjurySep 11, 2024Naturally Worn; Naturally Worn

  LEGAL CASE ¿ USA (MASTER CASE NO. (B)(4)). RELATED (B)(4) LH REV 1. (B)(4) LH REV 2. IT WAS REPORTED THAT APPROXIMATELY 166 MONTHS AFTER A TOTAL HIP REPLACEMENT PROCEDURE, THE PATIENT HAS EXPERIENCED PROSTHESIS WEAR, PAIN, SWELLING, INSTABILITY, OSTEOLYSIS. NO FURTHER ISSUES OR COMPLICATIONS WERE REPORTED. NO ADDITIONAL INFORMATION IS AVAILABLE." (B)(6) 132-28-06 - ACUMATCH 15 DEGREE LINER 28MM SZ F. ***SERIAL NUMBER (B)(6) IS CONFIRMED TO HAVE BEEN PACKAGED IN A VACUUM BAG THAT DOES CONTAIN EVOH AND WAS NOT AFFECTED BY THE RECALL.

  Patient problems: Joint Laxity; Osteolysis; Pain; Swelling/ Edema

  MAUDE report 20193831 ↗
• InjuryAug 5, 2021Naturally Worn; Naturally Worn

  AS REPORTED, SURGEON REVISED PATIENT DUE TO DISLOCATING. SURGEON NOTED THERE WAS SIGNIFICANT POLY WEAR WITH MINIMAL OSTEOLYSIS ON THE ACETABULUM. A NEW LINER WAS TRIALED IN ACUMATCH CUP BUT THE STABILITY HE WANTED WAS NOT ACHIEVED. THE CUP WAS REMOVED AND NEW ALTEON CUP WAS IMPLANTED. PATIENT HIP WAS STABLE WITH NEW IMPLANTS. PATIENT AS LEFT IN STABLE CONDITION. NO ADDITIONAL INFORMATION IS AVAILABLE.

  Patient problems: Joint Dislocation

  MAUDE report 12280792 ↗
• InjuryJun 19, 2020Naturally Worn; Naturally Worn

  AS REPORTED, APPROXIMATELY 19 ½ YEARS POSTOP THE INITIAL IMPLANT, THIS (B)(6) Y/O FEMALE PATIENT EXPERIENCED A LEFT HIP REVISION BECAUSE THE HIP FRACTURED. THE SURGEON BELIEVES THAT OSTEOLYSIS AND POLY WEAR LEAD TO A GRADUAL WEAKENING OF THE BONE AND EVENTUAL FRACTURE. THE HIP WAS REVISED DUE TO A PERI PROSTHETIC FRACTURE. THE SURGEON CHOSE TO REPLACE WITH COMPETITOR¿S DEVICES. IN ACCORDANCE WITH HOSPITAL POLICY WE ARE UNABLE TO RETURN EXPLANTS. PATIENT WAS LAST KNOWN TO BE IN STABLE CONDITION FOLLOWING THE EVENT. WEIGHT (B)(6) KGS AND NO ADDITIONAL MEDICAL HISTORY PROVIDED.

  Patient problems: Failure of Implant

  MAUDE report 10177018 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K993082. One submission often covers many models, so check the product and lot details in each record.

• Z-1031-2017 · Nov 7, 2016 · Terminated
  AcuMatch A-Series Connexion GXL Enhanced Polyethylene Acetabular Liner, 15, +5 mm Lateralized, 36 mm I.D., Size J.